Department of Pediatric Gastroenterology, Hepatology and Nutrition, MacKay Children's Hospital, Taipei, Taiwan; Department of Pediatrics, National Yang Ming Chiao Tung University Hospital, Yilan, Taiwan.
The Metabolomics Core Laboratory, Centers of Genomic and Precision Medicine, National Taiwan University, Taipei, Taiwan.
Pediatr Neonatol. 2022 Sep;63(5):468-473. doi: 10.1016/j.pedneo.2022.03.009. Epub 2022 May 18.
Omphalocele and gastroschisis are the two most common congenital abdominal wall defects; however, no previous study has focused on gastrointestinal and hepatobiliary tract malformations in these two conditions. This study aimed to investigate the demographic characteristics, coexisting congenital gastrointestinal and hepatobiliary tract anomalies, hospital course, and outcomes of patients with gastroschisis and omphalocele.
This is retrospective chart review of all patients admitted to one tertiary medical center in Taiwan between January 1, 2000 and June 30, 2020 with a diagnosis of gastroschisis or omphalocele. The medical records were reviewed to obtain demographic data regarding coexisting gastrointestinal and hepatobiliary tract anomalies and outcomes.
Of the 51 patients included, 21 had gastroschisis and 30 had omphalocele. Gastroschisis was associated with a significantly younger maternal age and a higher incidence of small for gestational age. Of the 30 patients with omphalocele, twelve had associated gastrointestinal and hepatobiliary anomalies. Seven of the 21 patients with gastroschisis had gastrointestinal anomalies, and none had hepatobiliary anomalies. Among the omphalocele patients, three (10%) had documented malrotation, and one developed midgut volvulus. Among gastroschisis patients, four patients (19%) had malrotation, and two developed midgut volvulus. There were no statistically significant differences in postoperative complications or mortality rates between those with and without gastrointestinal/hepatobiliary tract anomalies.
The diversity of coexisting gastrointestinal and hepatobiliary tract anomalies is higher in the omphalocele than in gastroschisis. In addition, we demonstrate that patients with gastroschisis or omphalocele have a higher rate of intestinal malrotation and midgut volvulus.
脐膨出和腹裂是两种最常见的先天性腹壁缺陷,但以前没有研究关注这两种疾病的胃肠道和肝胆道畸形。本研究旨在探讨腹裂和脐膨出患者的人口统计学特征、并存的先天性胃肠道和肝胆道异常、住院过程和结局。
这是对 2000 年 1 月 1 日至 2020 年 6 月 30 日期间在台湾一家三级医疗中心住院的所有被诊断为腹裂或脐膨出的患者的回顾性病历回顾。回顾病历以获取关于并存的胃肠道和肝胆道异常以及结局的人口统计学数据。
在 51 例患者中,21 例为腹裂,30 例为脐膨出。与脐膨出相比,腹裂的母亲年龄明显较小,胎儿生长受限的发生率较高。在 30 例脐膨出患者中,12 例存在胃肠道和肝胆道异常。21 例腹裂患者中有 7 例存在胃肠道异常,无一例存在肝胆道异常。在脐膨出患者中,有 3 例(10%)有记录的旋转不良,1 例发生中肠扭转。在腹裂患者中,有 4 例(19%)有旋转不良,2 例发生中肠扭转。在有或没有胃肠道/肝胆道异常的患者中,术后并发症或死亡率没有统计学差异。
脐膨出并存的胃肠道和肝胆道异常的多样性高于腹裂。此外,我们表明,腹裂和脐膨出患者的肠旋转不良和中肠扭转发生率较高。